2-Hydroxybenzylamine | CAS:932-30-9 | Manufacturer ChemFaces

2-Hydroxybenzylamine

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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.

Size /Price /Stock	10 mM * 1 mL in DMSO / $4.6 / In-stock
Other Packaging	*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap

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2-Hydroxybenzylamine Description

Source:	The herbs of Reseda odorata
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Structure Identification:

Chemistry, 2006,12(11): 3074–3081.

Task-Specific Ionic Liquids Bearing 2-Hydroxybenzylamine Units: Synthesis and Americium-Extraction Studies[Reference: WebLink]

The synthesis of two task-specific ionic liquids (TSILs) bearing 2-Hydroxybenzylamine entities is described.
METHODS AND RESULTS:
These compounds are based on an imidazolium substructure onto which one hydrobenzylamine-complexing moiety is grafted. We have demonstrated that, whether pure or diluted, TSIL is able to extract americium ions. Furthermore, recovery of americium from the IL phase into a receiving phase can be achieved under acidic conditions.
CONCLUSIONS:
A possible mechanism for the metal-ion partitioning is presented, in which the extraction system is driven by an ion-exchange mechanism.

International Journal of Quantum Chemistry,2010,10(12): 2179–2191.

Impact of the ionic forms on the UV–Vis spectra 2-hydroxybenzylamine. A TD-DFT study[Reference: WebLink]

METHODS AND RESULTS:
PCM-TD-DFT computations were used to examine the electronic transitions exhibited by the molecular species of 2-Hydroxybenzylamine (2-BNZ).
CONCLUSIONS:
The theoretical results thus obtained were found to accurately fit their experimental counterparts and to afford the assignation of the different experimental electronic transitions to 2-Hydroxybenzylamine tautomers present in the solution. Also, the HCTH functional was found to accurately reproduce electronic excitations in the cationic species and neutral tautomer, and the B3LYP functional to provide accurate predictions of the transitions for the anionic species and zwitterionic tautomer.

Product Name	2-Hydroxybenzylamine
Price:	$20 / 20mg
CAS No.:	932-30-9
Catalog No.:	CFN00079
Molecular Formula:	C₇H₉NO
Molecular Weight:	123.15 g/mol
Purity:	>=98%
Type of Compound:	Alkaloids
Physical Desc.:	Powder
Source:	The herbs of Reseda odorata
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS
Similar structural:	Comparison (Web) (SDF)
Guestbook:

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Antioxidants Compound Library Alkaloids Compound Library Sodium Channel Inhibitor Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	8.1202 mL	40.6009 mL	81.2018 mL	162.4036 mL	203.0045 mL
5 mM	1.624 mL	8.1202 mL	16.2404 mL	32.4807 mL	40.6009 mL
10 mM	0.812 mL	4.0601 mL	8.1202 mL	16.2404 mL	20.3004 mL
50 mM	0.1624 mL	0.812 mL	1.624 mL	3.2481 mL	4.0601 mL
100 mM	0.0812 mL	0.406 mL	0.812 mL	1.624 mL	2.03 mL

CFN00052	2-Amino-1-phenylethanol	111025-00-4	241.29	C₁₅H₁₅NO₂
CFN00053	N-Benzoyl-2-hydroxy-2-phenylethylamine	111059-46-2	241.29	C₁₅H₁₅NO₂
CFN00054	Muricatide	111025-01-5	283.33	C₁₇H₁₇NO₃
CFN00064	Benzylamine	100-46-9	107.15	C₇H₉N
CFN00065	N-Methylbenzylamine	103-67-3	121.18	C₈H₁₁N
CFN00079	2-Hydroxybenzylamine	932-30-9	123.15	C₇H₉NO
CFN00080	3-Hydroxybenzylamine	73604-31-6	123.15	C₇H₉NO
CFN00081	4-Hydroxybenzylamine	696-60-6	123.15	C₇H₉NO
CFN89344	Niazinin	147821-57-6	343.39	C₁₅H₂₁NO₆S
CFN89363	Niazimicin	147821-49-6	357.42	C₁₆H₂₃NO₆S